Ranging from literature monitoring and individual case safety reports to aggregate data reports, we will help you to ensure compliance with MDR 2017/745.
Rely on a professional team for all your case processing and literature assessment activities. Take advantage of our network of experienced medical advisors.
Through our aggregate data evaluation, facilitate development of your product portfolio. Use the acquired data in the best possible way.
We are dedicated to make responsible choices that balance economic, environmental, and social considerations, for a better future for all.
Our team can process all the data gathered through PMS activities whether it relates to quality complaints, ICSRs or literature articles. We have a multidisciplinary team to ensure quality assessment of information and in a timely manner.
We can help you ensure compliance with MDR 2017/745 with our medical writing department. Our advanced tools combined with experience will ensure that data is evaluated in the best possible way.
Adjusted to your therapeutic area
Medical device industry involves many different therapeutic areas. Our broad network of dedicated healthcare professionals and experts in their field stands at your disposal.